A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958824



Internal ID39858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155832749..155832800hg38UCSC Ensembl
chr4:156753901..156753952hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5413627
Supporting Variants
Samples
Known GenesASIC5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958824
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer